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Table 2 Summary of published CIITA SNP rs3087456 association studies in autoimmune disorders.

From: Lack of association of the CIITA-168A→G promoter SNP with myasthenia gravis and its role in autoimmunity

Study

Year

Population

Disease

Patients/Controls

Association

Swanberg, et. al. [4]

2005

Sweden

RA

1262/2506

p = 0.012

Swanberg, et. al. [4]

2005

Sweden

MS

520/2506

p = 0.028

Swanberg, et. al. [4]

2005

Sweden

MI

376/2506

p = 0.014

Koizuma et. al. [20]

2005

Japan

SLE

100/100

Not significant

Yazdani-Biuki et. al. [21]

2006

Austria

RA

362/1709

Not significant

Orozco et. al. [12]

2006

Spain

RA

748/676

p = 0.01a

Orozco et. al. [12]

2006

Sweden

RA

278/478

Not significant

Orozco et. al. [12]

2006

Argentina

RA

287/287

Not significant

Akkad et. al. [22]

2006

Germany

RA

319/463

Not significant

Akkad et. al. [22]

2006

Germany

MS

646/463

Not significant

Akkad et. al. [22]

2006

Germany

WGb

178/463

Not significant

Eyre et. al. [23]

2006

UK

RA

1401/2475

Not significant

Lindholm et. al. [24]

2006

Finland/Sweden

MI

1222/2345

Not significant

Ghaderi et. al. [16]

2006

Italy

AADc

128/406

p = 0.003

O'Doherty et. al. [25]

2007

Ireland

RA

293/316

Not significant

O'Doherty et. al. [25]

2007

Ireland

MS

440/316

Not significant

O'Doherty et. al. [25]

2007

Ireland

JIAd

74/316

Not significant

Linga-Reddy et. al. [17]

2007

Sweden

SLE

334/478

Not significant

Martinez et. al. [26]

2007

Spain

RA

350/519

Not significant

Martinez et. al. [26]

2007

Spain

MS

396/519

Not significant

Martinez et. al. [26]

2007

Spain

IBSe

663/519

Not significant

Iikuni et. al. [13]

2007

Japan

RA

1121/450

p = 0.003f

Harrison et. al. [27]

2007

UK

RA

733/613

Not significant

Sánchez et. al. [28]

2008

SLE

SLE

394/514

Not significant

Pan-Hammarström, et. al. [29]

2008

Sweden

CVIDg

97/1826

Not significant

Pan-Hammarström, et. al. [29]

2008

Sweden

IgADh

249/1826

Not significant

Skinningsrud, et. al. [15]

2008

Norway

AADc

332/1029

p = 0.044i

Dema et. al. [30]

2009

Spain

CDj

607/794

Not significant

Bronson, et. al. [19]

2010

USA/UK

MS

1320/1363

Not significant

  1. aConsidered by the authors to be a possible Type I error
  2. bWegener's granulomatosis
  3. cAutoimmune Addison's disease
  4. dJuvenile idiopathic arthritis
  5. eInflammatory bowel syndrome
  6. fAssociation with the major (A) rather than the minor allele of rs3087456
  7. gCommon variable immunodeficiency
  8. hIgA deficiency
  9. iUncorrected p-value in a study of 139 SNPs.
  10. jCeliac disease